WO2019157489A1 - Durable echogenic coatings for improving ultrasound visibility of medical devices - Google Patents
Durable echogenic coatings for improving ultrasound visibility of medical devices Download PDFInfo
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- WO2019157489A1 WO2019157489A1 PCT/US2019/017610 US2019017610W WO2019157489A1 WO 2019157489 A1 WO2019157489 A1 WO 2019157489A1 US 2019017610 W US2019017610 W US 2019017610W WO 2019157489 A1 WO2019157489 A1 WO 2019157489A1
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- Prior art keywords
- medical device
- coating
- hollow microspheres
- stainless
- durable
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- 238000000576 coating method Methods 0.000 title claims abstract description 46
- 238000002604 ultrasonography Methods 0.000 title claims abstract description 12
- 239000011248 coating agent Substances 0.000 claims abstract description 30
- 239000004005 microsphere Substances 0.000 claims abstract description 22
- 229920000642 polymer Polymers 0.000 claims abstract description 16
- 239000011159 matrix material Substances 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 239000011521 glass Substances 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 238000007598 dipping method Methods 0.000 claims 2
- 229920001296 polysiloxane Polymers 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 claims 1
- 150000003673 urethanes Chemical class 0.000 claims 1
- 229910001220 stainless steel Inorganic materials 0.000 description 27
- 239000010935 stainless steel Substances 0.000 description 27
- 239000000243 solution Substances 0.000 description 14
- 239000008199 coating composition Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 235000015277 pork Nutrition 0.000 description 5
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000012456 homogeneous solution Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005755 formation reaction Methods 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003791 organic solvent mixture Substances 0.000 description 2
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229940068984 polyvinyl alcohol Drugs 0.000 description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- MLHOXUWWKVQEJB-UHFFFAOYSA-N Propyleneglycol diacetate Chemical class CC(=O)OC(C)COC(C)=O MLHOXUWWKVQEJB-UHFFFAOYSA-N 0.000 description 1
- JABXMSSGPHGCII-UHFFFAOYSA-N acetic acid;propane-1,2-diol Chemical class CC(O)=O.CC(O)CO JABXMSSGPHGCII-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 210000003567 ascitic fluid Anatomy 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 210000004910 pleural fluid Anatomy 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/22—Echographic preparations; Ultrasound imaging preparations ; Optoacoustic imaging preparations
- A61K49/222—Echographic preparations; Ultrasound imaging preparations ; Optoacoustic imaging preparations characterised by a special physical form, e.g. emulsions, liposomes
- A61K49/223—Microbubbles, hollow microspheres, free gas bubbles, gas microspheres
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/0105—Steering means as part of the catheter or advancing means; Markers for positioning
- A61M25/0108—Steering means as part of the catheter or advancing means; Markers for positioning using radio-opaque or ultrasound markers
Definitions
- the present invention discloses methods for producing durable echogenic coatings for improving ultrasound visibility of medical devices.
- Ultrasound has been widely used to guide needle, catheter and guidewire placement and for vascular access, nerve blockade, drainage of pleural or ascitic fluid collections and percutaneous tracheostomy. Ultrasound allows identification of the target and collateral structures and real-time guidance to precisely place needles and other inserted devices.
- the echogenic coating is composed of multiple layers of coatings, in which two bubble generating elements (such as an acid and a carbonated base) are dispersed separately in two different layers of coatings; when the coatings are in contact with a fluid, these two bubble generating elements mix by diffusion and react with each other to form bubbles.
- two bubble generating elements such as an acid and a carbonated base
- US 2011/0104068 Al in which the two bubble generating elements are mixed together in one single layer of coating; they do not react with each other in anhydrous environment and they will react and generate bubbles when the coatings are in contact with an aqueous solution.
- the in situ bubble formation methods have some disadvantages: the echogenic effect is relatively short lived due to the escape of bubbles from the coatings to the environment; and the echogenic coatings are not durable due to the physical changes of the coatings caused by bubble formations, which can weaken the adherence of the coatings on the substrate surface.
- the present invention provides echogenic coatings that are stable and robust, that do not undergo physical changes during the usage of the coated needles and other devices.
- the coating composition of the present invention comprises a matrix formed by polymer and/or other materials dispersed with hollow microspheres.
- the polymers used in the coating composition preferably adhere strongly to the substrate surfaces and allow a homogeneous dispersion of the hollow microspheres.
- FIG. 1 is a drawing representing a substrate coated using subject invention durable echogenic coating comprising a polymer matrix and a dispersion of hollow microspheres.
- FIG. 2 shows the comparison of 2 ultrasonograms. The one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle immersed in water. The one on the right corresponds to the ultrasonogram of a coated stainless-steel needle immersed in water. The coated stainless-steel needle was prepared using the durable echogenic coating of the subject invention, as described in Example D.
- FIG. 3 shows the comparison of 2 ultrasonograms.
- the one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle inserted in a piece of pork.
- the one on the right corresponds to the ultrasonogram of a coated stainless-steel needle inserted in the same position of the same piece of pork.
- the coated stainless-steel needle was prepared using the durable echogenic coating of the subject invention, as described in Example D.
- the substrate which is the outer surface of a needle or other medical apparatus and/or devices, is coated with a matrix formed by polymer and/or other materials dispersed with hollow microspheres.
- the polymers used to form the polymer matrix preferably are biocompatible and have good tensile strength and adhesion to a wide array of metallic and polymeric substrates.
- Suitable polymers include those that have been used as polymeric coatings for medical devices such as polyurethane (PU), polymethylmethacrylate (PMMA), poly vinylalcohol (PVA), poly-N-vinylpyrrolidone (PVP), polyethylene oxide (PEO), and copolymers thereof. Mixtures and blends of these polymers also can be used. Other matrix based coatings or jackets can also be used.
- Hollow microspheres used to be dispersed in the polymer matrix preferably are biocompatible and have good tensile strength.
- Suitable hollow microspheres include hollow glass microsphere with diameter from 1 to 100 micrometers.
- the hollow microspheres and the polymers can be mixed together in one or more organic solvents to provide a coating composition.
- Suitable solvents that can be used include, but not limited to, tetrahydrofuran, acetone, methylethylketone, dimethylformamide, dimethyacetamide, ethylene carbonate, propylene carbonate, diglyme, N-methylpyrrolidone, ethyl acetate, ethylene and propylene glycol diacetates, alkyl ethers of ethylene and propylene glycol monoacetates, toluene, xylene and sterically hindered alcohols such as t-butanol and diacetone alcohol.
- the organic solvent or solvent mixture is evaporative.
- tetrahydrofuran can be used.
- the total solid loading can be between about 5 wt.% and about 30 wt.%, where the loading of the hollow microspheres is between about 1 wt.% and about 50 wt.% of that of the polymer.
- the medical device can be coated with the present coating composition.
- Various coating techniques such as spin coating, drop-casting, zone casting, dip coating, blade coating, and spraying can be used, depending on the shape of the medical device.
- the medical device can be an elongated member such as a catheter, a guidewire, or a needle, or a planar or spherical member such as an implant or a balloon.
- the thickness of the coating should be sufficient to entrap hollow microspheres having a diameter between about 1 pm and about 100 pm. Accordingly, typical thickness of the coating can range from about 0.01 mm to about 0.2 mm.
- the thickness achieved by one application of the coating composition will depend on the viscosity of the coating composition, the coating method, as well as the speed and the temperature at which the coating is applied. In some embodiments, multiple applications of the coating may be needed to build up the required thickness. The coating is then allowed to dry.
- Stainless-steel needles were coated with the subject invention method.
- a coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (11 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained.
- Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
- Stainless-steel needles were coated with the subject invention method.
- a coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (18 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained.
- Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
- Stainless-steel needles were coated with the subject invention method.
- a coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (30 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained.
- Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
- Stainless-steel needles were coated with the subject invention method.
- a coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (50 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained.
- Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
- FIG. 2 shows the comparison of 2 ultrasonograms.
- the one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle immersed in water.
- the one on the right corresponds to the ultrasonogram of a coated stainless-steel needle immersed in water.
- the coated needle has significantly improved ultrasound visibility compared to the uncoated needle.
- FIG. 2 shows the comparison of 2 ultrasonograms.
- the one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle inserted in a piece of pork.
- the one on the right corresponds to the ultrasonogram of a coated stainless-steel needle inserted in the same position of the same piece of pork.
- the coated needle has significantly improved ultrasound visibility compared to the uncoated needle.
- Stainless-steel needles prepared using the durable echogenic coating of the subject invention as described in Example A were tested for durability.
- the coated needles were soaked in water, 0.1 M hydrochloric acid solution (pH ⁇ 1), and 0.1 M sodium carbonate solution (pH ⁇ 8.5) for 1 hour respectively.
- the coatings remain intact after soaking.
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- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Radiology & Medical Imaging (AREA)
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- Physics & Mathematics (AREA)
- Acoustics & Sound (AREA)
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- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
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Abstract
The present invention discloses methods for producing durable echogenic coatings for improving ultrasound visibility of medical devices. The coating comprises a polymer matrix dispersed with hollow microspheres.
Description
DURABLE ECHOGENIC COATINGS FOR IMPROVING ULTRASOUND
VISIBILITY OF MEDICAL DEVICES
by
Cross-Reference to Related Application
[0001] This application claims priority of U.S. Provisional Patent Application No.
62/629,144, filed February 12, 2018, the entire contents of which are incorporated by reference herein.
Field of the Invention
[0002] The present invention discloses methods for producing durable echogenic coatings for improving ultrasound visibility of medical devices.
Background of the Invention
[0003] Ultrasound has been widely used to guide needle, catheter and guidewire placement and for vascular access, nerve blockade, drainage of pleural or ascitic fluid collections and percutaneous tracheostomy. Ultrasound allows identification of the target and collateral structures and real-time guidance to precisely place needles and other inserted devices.
[0004] The visibility of a needle or other inserted devices in ultrasound guided procedures is extremely important. Without accurate identification of the position of the needle it is possible that damage to collateral structures may occur. However, most medical devices have an acoustic impedance similar to that of the tissue into which the device is inserted. Consequently, visibility of the device can be poor and accurate placement can become extremely difficult.
[0005] Gases have much lower acoustic impedance than liquids and solids due to their high compressibility. Accordingly, gas bubbles have a high degree of ultrasonic visibility compared to organ tissues because of their large impedance difference. Some prior arts have used in situ bubble formation methods. For example, in US 7,235,052, the echogenic coating is composed of multiple layers of coatings, in which two bubble generating elements (such as an acid and a carbonated base) are dispersed separately in two different layers of coatings; when the coatings are in contact with a fluid, these two bubble generating elements mix by diffusion and react with each other to form bubbles. Another example is US 2011/0104068 Al, in which the two bubble generating elements are mixed together in one single layer of coating; they do not react with each other in anhydrous environment and they will react and generate bubbles when the coatings are in contact with an aqueous solution.
[0006] The in situ bubble formation methods have some disadvantages: the echogenic effect is relatively short lived due to the escape of bubbles from the coatings to the environment; and the echogenic coatings are not durable due to the physical changes of the coatings caused by bubble formations, which can weaken the adherence of the coatings on the substrate surface.
Summary of the Invention
[0007] In light of the foregoing, the present invention provides echogenic coatings that are stable and robust, that do not undergo physical changes during the usage of the coated needles and other devices. More specifically, the coating composition of the present invention comprises a matrix formed by polymer and/or other materials dispersed with hollow microspheres. The polymers used in the coating composition preferably adhere strongly to the substrate surfaces and allow a homogeneous dispersion of the hollow microspheres.
Brief Description of the Figures
[0008] FIG. 1 is a drawing representing a substrate coated using subject invention durable echogenic coating comprising a polymer matrix and a dispersion of hollow microspheres.
[0009] FIG. 2 shows the comparison of 2 ultrasonograms. The one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle immersed in water. The one on the right corresponds to the ultrasonogram of a coated stainless-steel needle immersed in water. The coated stainless-steel needle was prepared using the durable echogenic coating of the subject invention, as described in Example D.
[0010] FIG. 3 shows the comparison of 2 ultrasonograms. The one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle inserted in a piece of pork. The one on the right corresponds to the ultrasonogram of a coated stainless-steel needle inserted in the same position of the same piece of pork. The coated stainless-steel needle was prepared using the durable echogenic coating of the subject invention, as described in Example D.
Detailed Description of the Invention
[0011] With reference to FIG. 1, the substrate, which is the outer surface of a needle or other medical apparatus and/or devices, is coated with a matrix formed by polymer and/or other materials dispersed with hollow microspheres.
[0016] The polymers used to form the polymer matrix preferably are biocompatible and have good tensile strength and adhesion to a wide array of metallic and polymeric substrates. Suitable polymers include those that have been used as polymeric coatings for medical devices such as polyurethane (PU), polymethylmethacrylate (PMMA), poly vinylalcohol (PVA), poly-N-vinylpyrrolidone (PVP), polyethylene oxide (PEO), and copolymers thereof. Mixtures and blends of these polymers also can be used. Other matrix based coatings or jackets can also be used.
[0017] Hollow microspheres used to be dispersed in the polymer matrix preferably are biocompatible and have good tensile strength. Suitable hollow microspheres include hollow glass microsphere with diameter from 1 to 100 micrometers.
[0018] The hollow microspheres and the polymers can be mixed together in one or more organic solvents to provide a coating composition. Suitable solvents that can be used include, but not limited to, tetrahydrofuran, acetone, methylethylketone, dimethylformamide, dimethyacetamide, ethylene carbonate, propylene carbonate, diglyme, N-methylpyrrolidone, ethyl acetate, ethylene and propylene glycol diacetates,
alkyl ethers of ethylene and propylene glycol monoacetates, toluene, xylene and sterically hindered alcohols such as t-butanol and diacetone alcohol. In preferred embodiments, the organic solvent or solvent mixture is evaporative. For example, tetrahydrofuran can be used. The total solid loading can be between about 5 wt.% and about 30 wt.%, where the loading of the hollow microspheres is between about 1 wt.% and about 50 wt.% of that of the polymer.
[0019] To improve the echogenicity of a medical device, at least a portion of the surface of the medical device can be coated with the present coating composition. Various coating techniques such as spin coating, drop-casting, zone casting, dip coating, blade coating, and spraying can be used, depending on the shape of the medical device. For example, the medical device can be an elongated member such as a catheter, a guidewire, or a needle, or a planar or spherical member such as an implant or a balloon. The thickness of the coating should be sufficient to entrap hollow microspheres having a diameter between about 1 pm and about 100 pm. Accordingly, typical thickness of the coating can range from about 0.01 mm to about 0.2 mm. The thickness achieved by one application of the coating composition will depend on the viscosity of the coating composition, the coating method, as well as the speed and the temperature at which the coating is applied. In some embodiments, multiple applications of the coating may be needed to build up the required thickness. The coating is then allowed to dry.
EXAMPLES
Example A
[0020] Stainless-steel needles were coated with the subject invention method. A coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (11 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained. Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
Example B
[0021] Stainless-steel needles were coated with the subject invention method. A coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (18 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained. Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
Example C
[0022] Stainless-steel needles were coated with the subject invention method. A coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (30 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained. Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
Example D
[0023] Stainless-steel needles were coated with the subject invention method. A coating solution was prepared by first dissolving 5% (w/v) ChronoFlex AL in tetrahydrofuron, followed by mixing 2% (w/v) hollow glass microspheres (50 pm diameter) in the ChronoFlex solution until a homogeneous solution is obtained. Stainless-steel needles were then dipped into the coating solution and lifted up slowly. The stainless-steel needles were then dried at room temperature for 30 minutes.
Example E
[0024] Stainless-steel needles prepared using the durable echogenic coating of the subject invention as described in Example D were compared with uncoated stainless-steel needles for ultrasound visibility in water. FIG. 2
shows the comparison of 2 ultrasonograms. The one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle immersed in water. The one on the right corresponds to the ultrasonogram of a coated stainless-steel needle immersed in water. The coated needle has significantly improved ultrasound visibility compared to the uncoated needle.
Example F
[0025] Stainless-steel needles prepared using the durable echogenic coating of the subject invention as described in Example A were compared with uncoated stainless-steel needles for ultrasound visibility when they were inserted in a piece of pork. FIG. 2 shows the comparison of 2 ultrasonograms. The one on the left corresponds to the ultrasonogram of an uncoated stainless-steel needle inserted in a piece of pork. The one on the right corresponds to the ultrasonogram of a coated stainless-steel needle inserted in the same position of the same piece of pork. The coated needle has significantly improved ultrasound visibility compared to the uncoated needle.
Example G
[0026] Stainless-steel needles prepared using the durable echogenic coating of the subject invention as described in Example A were tested for durability. The coated needles were soaked in water, 0.1 M hydrochloric acid solution (pH ~ 1), and 0.1 M sodium carbonate solution (pH ~ 8.5) for 1 hour respectively. The coatings remain intact after soaking.
[0027] The present teachings can be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative rather than limiting on the present teachings described herein. The scope of the present teachings is thus indicated by the
appended claims rather than by the foregoing description, and all changes that come within the meaning and range of equivalency of the claims are intended to be embraced therein.
Claims
1. A medical device comprising a coating for improving ultrasound visibility, wherein the coating comprises hollow microspheres dispersed within a polymer matrix.
2. A medical device of Claim 1, wherein the polymer matrix includes polyurethanes.
3. A medical device of Claim 1, wherein the polymer matrix includes polycarbonate- based urethanes.
4. A medical device of Claim 1, wherein the polymer includes silicones.
5. A medical device of Claim 1, wherein the hollow microspheres include glass microspheres.
6. A medical device of Claim 1, wherein the hollow microspheres have a diameter between 1 to 100 micrometers.
7. A medical device of Claim 1, wherein the weight-to-weight ratio of hollow microspheres to matrix is between 0.1 to 10.
8. A medical device of Claim 1, wherein the coating is prepared by dipping the substrate in the coating solution containing the matrix and the hollow microspheres.
9. A medical device of Claim 8, wherein the coating solution contains 0.1 - 20% (weight to volume) of the combined matrix and hollow microspheres.
10. A medical device of Claim 8, wherein the solvent is either tetrahydrofuran, dimethylacetamide, or a mixture of both.
11 A medical device of Claim 8, wherein a multiple dipping process is used to obtain the coating.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862629144P | 2018-02-12 | 2018-02-12 | |
US62/629,144 | 2018-02-12 |
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US5201314A (en) * | 1989-03-09 | 1993-04-13 | Vance Products Incorporated | Echogenic devices, material and method |
US20020151796A1 (en) * | 2001-02-09 | 2002-10-17 | Edouard Koulik | Echogenic devices and methods of making and using such devices |
US6506156B1 (en) * | 2000-01-19 | 2003-01-14 | Vascular Control Systems, Inc | Echogenic coating |
US20040077948A1 (en) * | 1996-11-06 | 2004-04-22 | Sts Biopolymers, Inc. | Echogenic coatings with overcoat |
US20100239505A1 (en) * | 2009-03-17 | 2010-09-23 | Ruger Medical Gmbh | Apparatus with an echogenic coating and echogenic layer |
US20130204232A1 (en) * | 2012-01-13 | 2013-08-08 | Juergen Wieser | Unknown |
US20140207000A1 (en) * | 2011-04-26 | 2014-07-24 | Encapson B.V. | Coating for improving the ultrasound visibility |
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US5201314A (en) * | 1989-03-09 | 1993-04-13 | Vance Products Incorporated | Echogenic devices, material and method |
US5133742A (en) * | 1990-06-15 | 1992-07-28 | Corvita Corporation | Crack-resistant polycarbonate urethane polymer prostheses |
US20040077948A1 (en) * | 1996-11-06 | 2004-04-22 | Sts Biopolymers, Inc. | Echogenic coatings with overcoat |
US6506156B1 (en) * | 2000-01-19 | 2003-01-14 | Vascular Control Systems, Inc | Echogenic coating |
US20020151796A1 (en) * | 2001-02-09 | 2002-10-17 | Edouard Koulik | Echogenic devices and methods of making and using such devices |
US20100239505A1 (en) * | 2009-03-17 | 2010-09-23 | Ruger Medical Gmbh | Apparatus with an echogenic coating and echogenic layer |
US20140207000A1 (en) * | 2011-04-26 | 2014-07-24 | Encapson B.V. | Coating for improving the ultrasound visibility |
US20130204232A1 (en) * | 2012-01-13 | 2013-08-08 | Juergen Wieser | Unknown |
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